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A0627

Sigma-Aldrich

Adenosine-5′-diphosphoglucose disodium salt

≥93%

Sinónimos:

ADP, ADP-Glucose, ADP-glc, ADPG

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About This Item

Fórmula empírica (notación de Hill):
C16H23N5Na2O15P2
Número de CAS:
102129-65-7
Peso molecular:
633.31
Número MDL:
MFCD00056005
Código UNSPSC:
41106305
ID de la sustancia en PubChem:
24890440
NACRES:
NA.51

origen biológico

yeast

Nivel de calidad

200

Análisis

≥93%

formulario

powder

temp. de almacenamiento

−20°C

cadena SMILES

[Na+].[Na+].Nc1ncnc2n(cnc12)[C@@H]3O[C@H](COP([O-])(=O)OP([O-])(=O)OC4O[C@H](CO)[C@@H](O)[C@H](O)[C@H]4O)[C@@H](O)[C@H]3O

InChI

1S/C16H25N5O15P2.2Na/c17-13-7-14(19-3-18-13)21(4-20-7)15-11(26)9(24)6(33-15)2-32-37(28,29)36-38(30,31)35-16-12(27)10(25)8(23)5(1-22)34-16;;/h3-6,8-12,15-16,22-27H,1-2H2,(H,28,29)(H,30,31)(H2,17,18,19);;/q;2*+1/p-2/t5-,6-,8-,9-,10+,11-,12-,15-,16?;;/m1../s1

Clave InChI

GZBIVALVIPYODS-UQGWVDHFSA-L

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Aplicación

Adenosine-5′-diphosphoglucose (ADP-Glucose) is a substrate widely used as a glucose donor. It is a substrate in starch synthesis by starch synthase (EC 2.4.1.21). ADP-Glucose is a substrate for alpha-1,4-glucan-protein synthase (ADP-forming) (EC 2.4.1.113), ADP-glucose pyrophosphorylases and many glucosyltransferases.
Adenosine-5′-diphosphoglucose disodium salt has been used as a component of the reaction mixture to measure the enzymatic activity of adenosine-5′-diphosphate (ADP)-glucose pyrophosphorylase (AGPase) and for the synthesis of starch.

Acciones bioquímicas o fisiológicas

Adenosine-5′-diphosphoglucose (ADP-Glucose) is a substrate widely used as a glucose donor. It is a substrate starch synthase (EC 2.4.1.21) in starch synthesis. ADP-glucose is a substrate for α-1,4-glucan-protein synthase (ADP-forming) (EC 2.4.1.113), ADP-glucose pyrophosphorylases and many glucosyltransferases.

Código de clase de almacenamiento

11 - Combustible Solids

Clase de riesgo para el agua (WGK)

WGK 3

Punto de inflamabilidad (°F)

Not applicable

Punto de inflamabilidad (°C)

Not applicable

Equipo de protección personal

Eyeshields, Gloves, type N95 (US)

Certificados de análisis (COA)

Busque Certificados de análisis (COA) introduciendo el número de lote del producto. Los números de lote se encuentran en la etiqueta del producto después de las palabras «Lot» o «Batch»

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Mengyao Xue et al.
Rice (New York, N.Y.), 12(1), 100-100 (2020-01-01)
The endosperm of rice (Oryza sativa) has been usually used for the study of starch synthesis. Although several related factors have been revealed, other unknown members remain to be identified, given that starch synthesis is a complicated and sophisticated process.
Mai Nagatoshi et al.
The Journal of biological chemistry, 286(37), 32866-32874 (2011-07-30)
Iridoids are one of the most widely distributed secondary metabolites in higher plants. They are pharmacologically active principles in various medicinal plants and key intermediates in the biosynthesis of monoterpenoid indole alkaloids as well as quinoline alkaloids. Although most iridoids
José G Vallarino et al.
Scientific reports, 10(1), 17219-17219 (2020-10-16)
The capacity to assimilate carbon and nitrogen, to transport the resultant sugars and amino acids to sink tissues, and to convert the incoming sugars and amino acids into storage compounds in the sink tissues, are key determinants of crop yield.
Steven Ball et al.
Journal of experimental botany, 62(6), 1775-1801 (2011-01-12)
Solid semi-crystalline starch and hydrosoluble glycogen define two distinct physical states of the same type of storage polysaccharide. Appearance of semi-crystalline storage polysaccharides appears linked to the requirement of unicellular diazotrophic cyanobacteria to fuel nitrogenase and protect it from oxygen
Extraction and assays of ADP-glucose pyrophosphorylase, soluble starch synthase and granule bound starch synthase from wheat (Triticum aestivum L.) Grains
Kulichikhin K, et al.
Bio-protocol, 6(e1929) (2016)
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